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2-Hydroxy-4-pyridinecarboxaldehyde, also known as 4-Pyridinecarboxaldehyde, 2-hydroxy-, is a chemical compound with the molecular formula C6H5NO2. It is a light yellow to brown powder that serves as a versatile building block in the synthesis of various compounds.

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  • 188554-13-4 Structure
  • Basic information

    1. Product Name: 2-HYDROXY-4-PYRIDINECARBOXALDEHYDE
    2. Synonyms: 2-HYDROXY-4-PYRIDINECARBOXALDEHYDE;2-HYDROXY-4-FORMYLPYRIDINE;2-HYDROXY-PYRIDINE-4-CARBALDEHYDE;2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE;4-Pyridinecarboxaldehyde,1,2-dihydro-2-oxo-(9CI);2-AMINO-5-(AMINOMETHYL)-4-METHYLTHIAZOLE;2-Hydroxyisonicotinaldehyde;2-Oxo-1,2-dihydro-pyridine-4-carbaldehyde
    3. CAS NO:188554-13-4
    4. Molecular Formula: C6H5NO2
    5. Molecular Weight: 123.11
    6. EINECS: N/A
    7. Product Categories: PYRIDINE;pharmacetical;API intermediates;Pyridines;Heterocycle-Pyridine series
    8. Mol File: 188554-13-4.mol
  • Chemical Properties

    1. Melting Point: 79-81 °C
    2. Boiling Point: 333.7 °C at 760 mmHg
    3. Flash Point: 175.1 °C
    4. Appearance: /
    5. Density: 1.365 g/cm3
    6. Vapor Pressure: 0.000341mmHg at 25°C
    7. Refractive Index: 1.647
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. PKA: 11.17±0.10(Predicted)
    11. CAS DataBase Reference: 2-HYDROXY-4-PYRIDINECARBOXALDEHYDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-HYDROXY-4-PYRIDINECARBOXALDEHYDE(188554-13-4)
    13. EPA Substance Registry System: 2-HYDROXY-4-PYRIDINECARBOXALDEHYDE(188554-13-4)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-36-43
    3. Safety Statements: 26-36/37
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 188554-13-4(Hazardous Substances Data)

188554-13-4 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-Hydroxy-4-pyridinecarboxaldehyde is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique chemical structure allows for the development of new drugs and pesticides with improved efficacy and safety profiles.
Used in Dye and Pigment Production:
This chemical compound is also utilized in the production of dyes and pigments, contributing to the coloration of various materials and products. Its light yellow to brown color can be modified through chemical reactions to create a wide range of hues.
Used in Organic Compound Manufacturing:
2-Hydroxy-4-pyridinecarboxaldehyde serves as an intermediate in the manufacturing of other organic compounds, expanding its applications across different industries. Its versatility in chemical reactions enables the creation of new compounds with diverse properties and uses.
Safety Precautions:
While 2-Hydroxy-4-pyridinecarboxaldehyde has numerous applications, it is essential to handle the chemical with caution and implement proper safety measures during its use and storage. This ensures the protection of both the environment and the individuals involved in its production and application processes.

Check Digit Verification of cas no

The CAS Registry Mumber 188554-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,5,5 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 188554-13:
(8*1)+(7*8)+(6*8)+(5*5)+(4*5)+(3*4)+(2*1)+(1*3)=174
174 % 10 = 4
So 188554-13-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9N3S/c1-3-4(2-6)9-5(7)8-3/h2,6H2,1H3,(H2,7,8)

188554-13-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-1H-pyridine-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Hydroxyisonicotinaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:188554-13-4 SDS

188554-13-4Relevant articles and documents

Photochemical synthesis of benz[h]isoquinolines

Abbott, Belinda M.,Ferrari, Frank D.,Harnor, Suzannah J.,Barnes, John C.,Marquez, Rodolfo

, p. 5072 - 5078 (2008/09/21)

The synthesis of benz[h]isoquinolines has been achieved using a highly convergent photochemical method. The approach presented provides ready access to biologically active compounds and building blocks not readily available through other methods.

INHIBITORS OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE, AND COMPOSITIONS AND TREATMENTS USING THE SAME

-

Page 132, (2008/06/13)

The invention relates to compounds of the formula (I) and to pharmaceutically acceptable salts, solvates, prodrugs and metabolites thereof, wherein W, Z, R1and R2, are as defined herein. The invention also relates to methods of treating Hepatitis C virus in mammals by administering the compounds of formula (I), and to pharmaceutical compositions for treating such disorders, which contain the compounds of formula (I). The invention also relates to methods of preparing the compounds of formula (I).

N-aryl(thio)anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors

-

, (2008/06/13)

Described are compounds of formula (I), wherein W is O or S; X is NR8; Y is CR9R10-(CH2)n wherein R9 and R10 are independently of each other hydrogen or lower alkyl, and n is an integer of

Fluorescent pigments of the retinal pigment epithelium and age-related macular degeneration

Ben-Shabat, Shimon,Parish, Craig A.,Hashimoto, Masaru,Liu, Jianghua,Nakanishi, Koji,Sparrow, Janet R.

, p. 1533 - 1540 (2007/10/03)

The major hydrophobic fluorophore of the retinal pigment epithelium (RPE) is A2E, a pyridinium bis-retinoid derived from all-trans-retinal and phosphatidyl-ethanolamine. The accumulation of fluorophores such as A2E is implicated in the pathogenesis of age-related macular degeneration (AMD), a disease associated with the deterioration of central vision and a leading cause of blindness in the elderly. Recent chemical and biological studies have provided insight into the synthesis and biosynthesis of A2E, the spectroscopic properties of this pigment, and the role of A2E and RPE cell death.

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